FDA 483 - Philips Ultrasound, Inc. - January 31, 2025
FDA 483 for Philips Ultrasound, Inc. on January 31, 2025. Product: device. Access full analysis and detailed observations.
One-time purchase from the GKS catalog. Lifetime access in your library. Single documents and full company profiles available. All sales final.
FDA 483 for Philips Ultrasound, Inc. on January 31, 2025. Product: device. Access full analysis and detailed observations.
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Company
Philips Ultrasound, Inc.Inspection Date
January 31, 2025
Product Type
device
Office
Seattle District OfficeID: be863243-a266-405f-8136-dbb77875e232
View on DashboardTransform Regulatory Data into Actionable Intelligence
Join leading pharmaceutical and medical device companies who trust GKS for their regulatory compliance needs.
Try KeyPedia Today
Explore our real use cases and discover our features in depth.
Subscribe to our newsletter
Get the latest updates and insights delivered to your inbox